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BioWorld - Sunday, December 7, 2025
Home » Newsletters » BioWorld Science

BioWorld Science

Dec. 15, 2016

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Shanghai Institute Materia Medica develops tyrosine kinase inhibitors

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ExpreS2ion and Abivax enter collaboration on Ebola prophylaxis and treatment program

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Medicenna Biopharma begins phase II study of MDNA-55

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European Commission grants conditional approval to Ocaliva

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KemPharm reports positive results from phase I proof-of-concept study of d-MPH prodrug

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ALS symptoms deteriorate after stopping ibudilast treatment in clinical trial

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AN-13762 described as representing a new class of antimalarial

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Novel therapeutic targets described at the Society for Neuroscience Annual Meeting

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Concert Pharmaceuticals completes phase I study of JAK inhibitor for alopecia areata

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TPC-064: a novel mutant-selective EGFR inhibitor

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vTv Therapeutics reports topline data from phase II trial of TTP-273 in type 2 diabetes

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Kiadis obtains U.K. approvals for phase I/II trial of ATIR-201 for thalassemia

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FDA gives orphan drug designation to nintedanib in mesothelioma

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Encouraging results reported from tolerability proof-of-concept study of KarXT

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Epigenetic compound CTI-309 shows promise as Alzheimer's disease candidate

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TSRI, Icahn School of Medicine and UPenn patent nAChR modulators

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Bicycle Therapeutics collaborates with Cancer Research UK to study BT-1718

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Harvard and Evotec divulge novel bacterial glycosyl transferase inhibitors

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Merck & Co. discovers soluble guanylate cyclase activators

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FDA approves Eucrisa for atopic dermatitis

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Principia Biopharma patents new FGFR inhibitors

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Chong Kun Dang Holdings divulges new histone deacetylase inhibitors

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Hologic to divest blood screening business to Grifols

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argenx initiates phase I/II study of ARGX-110 with azacitidine in newly diagnosed AML

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Third Rock Ventures launches Goldfinch Bio with a focus on therapies for kidney disease

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Biogen files for Japanese approval of nusinersen for SMA

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Lonza set to acquire Capsugel

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CM-4620 receives EMA orphan designation for acute pancreatitis

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Gamunex-C granted FDA orphan status for myasthenia gravis

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Polatuzumab vedotin given U.S. orphan drug designation

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